Extended Data Fig. 1: Quantification of UvrABD binding to RNAP in vivo.
From: Crucial role and mechanism of transcription-coupled DNA repair in bacteria

Supplementary to Fig. 1. a, UV sensitivity of E. coli strains used in Fig. 1. Representative efficiencies of colony formation of parent wild-type (MG1655) and mutant E. coli cells exposed to the indicated UV doses. Overnight cultures were diluted 1:100 with fresh LB and grown to ~ 2x107. Cells were serially diluted, plated on LB agar, irradiated with UV, and incubated at 37 °C for 24 h. b, Representative western blots used to generate the plots of Fig. 1b–d. c, Quantitative mass-spectrometry analysis of RNAP-associated UvrABD, Mfd, and Rho in the exponentially grown cells prior to genotoxic stress. RNAP pulldown samples were prepared as in Fig. 1. Values are normalized to that of NusA-containing RNAPs, thus reflecting the RNAP molecules engaged in elongation in vivo.